Precursors of many secreted and cell surface proteins contain NH2-terminal
signal sequences that lead proteins into the endoplasmic reticulum and to t
he cell surface. Methods have been developed to clone and identify such pro
teins by trapping their NH2-terminal signal sequences, so called signal seq
uence traps. In this study we present an alternative and simplified signal
sequence trap based on the combination of a novel vector construct expressi
ng a cDNA library in fusion with a CD19 reporter gene, transfection in mamm
alian cells and selection of cells expressing trapped signal sequences usin
g magnetic beads. Using this method we have isolated several known and nove
l factors with signal peptides.